European CE Marking Process for Medical Device Course

The course goal is to provide you with the right skills to follow the right path in getting the CE mark for your products. It covers all the areas of knowledge that a person needs such as having a greater insight into the overall regulatory process of registering medical devices in Europe and obtaining a CE mark and many more. The course uses different ways of delivering knowledge like case studies, videos, exercises, and individual tests. At the completion of the course, the skills that YOU will have are practical, applicable, and implementable.